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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Circulation (New York, N.Y.), 2010-02, Vol.121 (5), p.635-643

2010

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Dysfonctions sinusales : mécanismes physiopathologiques

Archives des maladies du coeur et des vaisseaux. Pratique, 2012-11, Vol.2012 (212), p.27-30

Le Marec, H.

2012

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Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Europace (London, England), 2013-12, Vol.15 (12), p.1805-1811

2013

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Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Biochimica et biophysica acta, 2014-02, Vol.1843 (2), p.234-244

2014

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G024 Implication des canaux KATP dans le syndrome de repolarisation précoce

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S71

2009

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Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

Heart rhythm, 2008-11, Vol.5 (11), p.1561-1564

2008

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Cardiac conduction defects associate with mutations in SCN5A

Nature genetics, 1999-09, Vol.23 (1), p.20-21

1999

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GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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Génétique de la fibrillation auriculaire

Annales de cardiologie et d'angéiologie, 2009-12, Vol.58, p.S70-S72

2009

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Actualité sur la génétique du prolapsus valvulaire mitral

Archives des maladies du coeur et des vaisseaux. Pratique, 2014-12, Vol.2014 (233), p.28-30

2014

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The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

Journal of medical genetics, 2003-02, Vol.40 (2), p.141-145

2003

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Do inherited prothrombotic factors have a role in myocardial infarction with normal coronary arteriogram?

Journal of internal medicine, 1998-12, Vol.244 (6), p.543-544

1998

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Nature (London), 2003-02, Vol.421 (6923), p.634-639

2003

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Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization

Neurology, 2003-01, Vol.60 (2), p.340

2003

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P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

Circulation (New York, N.Y.), 2001-12, Vol.104 (25), p.3081-3086

2001

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Alterations in the force‐frequency relationship by tert‐ butylbenzohydroquinone, a putative SR Ca2+ pump inhibitor, in rabbit and rat ventricular muscle

British journal of pharmacology, 1996-01, Vol.117 (2), p.258-267

1996

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P5441Aortic valve phenotype associated with filamin-A mutations: a comprehensive echocardiographic and outcomes analyses

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S70

2009

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Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Journal of the American College of Cardiology, 2003-02, Vol.41 (4), p.643-652

2003

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Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

European heart journal, 2001-03, Vol.22 (5), p.410-422

2001

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Familial aggregation of calcific aortic valve stenosis in the western part of France

Circulation (New York, N.Y.), 2006-02, Vol.113 (6), p.856-860

2006

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Early after/depolarizations and triggered activity: mechanisms and autonomic regulation

Fundamental & clinical pharmacology, 1993-02, Vol.7 (1), p.39-49

1993

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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Dysfonctions sinusales : mécanismes physiopathologiques

Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

G024 Implication des canaux KATP dans le syndrome de repolarisation précoce

Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

Cardiac conduction defects associate with mutations in SCN5A

GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Génétique de la fibrillation auriculaire

Actualité sur la génétique du prolapsus valvulaire mitral

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

Do inherited prothrombotic factors have a role in myocardial infarction with normal coronary arteriogram?

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization

P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

Alterations in the force‐frequency relationship by tert‐ butylbenzohydroquinone, a putative SR Ca2+ pump inhibitor, in rabbit and rat ventricular muscle

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study

P5441Aortic valve phenotype associated with filamin-A mutations: a comprehensive echocardiographic and outcomes analyses

G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

Familial aggregation of calcific aortic valve stenosis in the western part of France

Early after/depolarizations and triggered activity: mechanisms and autonomic regulation

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